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British Journal of Haematology|January 30, 2018
How I manage red cell transfusions in patients with sickle cell diseaseDavid C Rees, Susan Robinson, Jo HowardBritish Journal of Haematology|September 7, 2023
The cation-leaky hereditary stomatocytosis syndromes: A tale of six proteinsGordon W Stewart, John S Gibson, David C ReesHemasphere|August 24, 2022
Precision Medicine and Sickle Cell DiseaseSara El Hoss, Wassim El Nemer, David C ReesTrends in Pharmacological Sciences|March 31, 2012
Experiences in fragment-based drug discoveryChristopher W Murray, Marcel L Verdonk, David C ReesBMJ Paediatrics Open|November 7, 2018
High body mass index in children with sickle cell disease: a retrospective single-centre auditRachael Hall, Kate Gardner, David C Rees, et al.Lancet (London, England)|December 7, 2010
Sickle-cell diseaseDavid C Rees, Thomas N Williams, Mark T GladwinBritish Journal of Haematology|December 17, 2016
Update review of the acute porphyriasPenelope E Stein, Michael N Badminton, David C ReesHemoglobin|October 6, 2021
Pitfalls in the Diagnosis of β-Thalassemia IntermediaShiromi Perera, Angela Allen, David C Rees, et al.Organic & Biomolecular Chemistry|January 8, 2016
Design and synthesis of dihydroisoquinolones for fragment-based drug discovery (FBDD)Nick Palmer, Torren M Peakman, David Norton, et al.RSC Medicinal Chemistry|December 23, 2022
Introduction to the themed collection on fragment-based drug discoveryDavid C Rees, Anna K H Hirsch, Daniel A ErlansonPageof 14